Lucey D R, Novak J M, Polonis V R, Liu Y, Gartner S
Department of Retroviral Research, Walter Reed Army Institute of Research, Rockville, Maryland 20850, USA.
Clin Diagn Lab Immunol. 1994 May;1(3):330-5. doi: 10.1128/cdli.1.3.330-335.1994.
Substance P (SP), a member of the tachykinin family of neuropeptides, can immunomodulate human T cells and monocytes. SP has been shown to stimulate human monocytes to produce inflammatory cytokines and superoxide ions, and it enhances tumoricidal activity in vitro. A specific SP receptor, however, has not been identified on human monocytes/macrophages. In this study, we report that 125I-SP binds to human monocytes/macrophages with high affinity and specificity (Kd = 2.7 x 10(-8) to 5.5 x 10(-8) M). Our measurements of binding affinity to this single class of receptors were possible only when experiments were performed in the presence of excess serine proteinase inhibitor (serpin) enzyme complex receptor ligand. We determined that 125I-SP bound to a specific receptor on human monocytes/macrophages and that this binding was detectable as early as 6 h and was maintained throughout 6 to 8 weeks in culture. Modulation of the diverse immunological and inflammatory effects of SP on human monocytes may be mediated through this specific SP receptor.
P物质(SP)是神经肽速激肽家族的成员之一,可对人类T细胞和单核细胞进行免疫调节。研究表明,SP能刺激人类单核细胞产生炎性细胞因子和超氧离子,并在体外增强其杀肿瘤活性。然而,尚未在人类单核细胞/巨噬细胞上鉴定出特异性的SP受体。在本研究中,我们报告125I-SP以高亲和力和特异性(解离常数Kd = 2.7×10(-8)至5.5×10(-8) M)与人类单核细胞/巨噬细胞结合。只有在过量丝氨酸蛋白酶抑制剂(丝氨酸蛋白酶抑制剂)酶复合受体配体存在的情况下进行实验,我们才能够测量与这一单类受体的结合亲和力。我们确定125I-SP与人类单核细胞/巨噬细胞上的特异性受体结合,这种结合最早在6小时即可检测到,并在培养6至8周的时间内持续存在。SP对人类单核细胞的多种免疫和炎症作用的调节可能是通过这种特异性SP受体介导的。